Bakhmutova Ekaterina V, Ouyang Xiang, Medvedev Dmitri G, Clearfield Abraham
Department of Chemistry, Texas A&M University, College Station, Texas 77843-3255.
Inorg Chem. 2003 Nov 3;42(22):7046-51. doi: 10.1021/ic0301425.
Novel cobalt phosphonates [Co(H(2)O)(4)(H(4)L)][H(2)L].2H(2)O, 1, and Co(2)(H(2)O)(2)(L), 2, have been synthesized from 1,8-octylenediphosphonic acid (H(4)L). 1 has been fully characterized by X-ray single-crystal data, TGA, IR spectroscopy, and chemical analysis. The compound crystallizes in the triclinic space group P1 with a = 5.5415(8) A, b = 8.6382(8) A, c = 16.794 (2) A, alpha = 87.694(2) degrees, beta = 80.859(2) degrees, gamma = 76.005(2) degrees, V = 770.11(19) A(3), and Z = 1. A cobalt atom lies in the center of symmetry and is octahedrally coordinated by two oxygen atoms from two undissociated diphosphonic ligands H(4)L and four molecules of water. The cobalt atom and undissociated ligand H(4)L are combined to form polymeric chains along the c-axis, resulting in the formation of a one-dimensional framework. The positive charge on the cobalt atom remains upon coordination and is balanced by a negatively charged uncoordinated ligand (H(2)L) found as a clathrate in the lattice. Two lattice water molecules, hydrogen-bonded with the coordinated and uncoordinated ligands, complete the structure. The metal phosphonate chains are held together and bridge the uncoordinated anionic ligands by a number of strong hydrogen bonds, which make the structure possible. Cobalt phosphonate 2 has been characterized by TGA measurements, IR spectroscopy, and chemical analysis. The compound has a layered structure with an interlayer spacing of 14.26 A. Metal phosphonate layers are cross-linked by hydrocarbon chains. The water molecules are coordinated to the metal atom. According to IR data, compound 2 contains two equivalent PO bonds and one different PO bond, which may be a result of the different types of Co-O-P connectivity within one phosphonic group.
新型钴膦酸盐[Co(H₂O)₄(H₄L)][H₂L]·2H₂O(1)和Co₂(H₂O)₂(L)(2)已由1,8 - 辛二膦酸(H₄L)合成。1已通过X射线单晶数据、热重分析(TGA)、红外光谱和化学分析进行了全面表征。该化合物结晶于三斜晶系空间群P1中,a = 5.5415(8) Å,b = 8.6382(8) Å,c = 16.794(2) Å,α = 87.694(2)°,β = 80.859(2)°,γ = 76.005(2)°,V = 770.11(19) ų,Z = 1。一个钴原子位于对称中心,由来自两个未解离的二膦酸配体H₄L的两个氧原子和四个水分子进行八面体配位。钴原子与未解离的配体H₄L结合,沿c轴形成聚合物链,从而形成一维骨架。钴原子配位后仍带有正电荷,并由晶格中作为笼形物存在的带负电荷的未配位配体(H₂L)平衡。两个晶格水分子通过氢键与配位和未配位的配体相连,完善了结构。金属膦酸盐链通过一些强氢键结合在一起,并桥连未配位的阴离子配体,这使得该结构得以形成。钴膦酸盐2已通过热重分析测量(TGA)、红外光谱和化学分析进行了表征。该化合物具有层状结构,层间距为14.26 Å。金属膦酸盐层由烃链交联。水分子与金属原子配位。根据红外数据,化合物2包含两个等效的P - O键和一个不同的P - O键,这可能是由于一个膦酸基团内不同类型的Co - O - P连接性导致的。